Jeremy M. Sage

Optical production of ultracold polar molecules

We demonstrate the production of ultracold polar RbCs molecules in their vibronic ground state, via photoassociation of laser-cooled atoms followed by a laser-stimulated state transfer process. The resulting sample of X1Sigma+ (nu = 0) molecules has a translational temperature of approximately 100 microK and a narrow distribution of rotational states. With the method described here it should be possible to produce samples even colder in all degrees of freedom, as well as other bialkali species.

Production and state-selective detection of ultracold RbCs molecules.

Using resonance-enhanced two-photon ionization, we detect ultracold, ground-state RbCs molecules formed via photoassociation in a laser-cooled mixture of 85Rb and 133Cs atoms. We obtain extensive bound-bound excitation spectra of these molecules, which provide detailed information about their vibrational distribution, as well as spectroscopic data on the RbCs ground a^3\Sigma^+ and excited (2)^3\Sigma^+, (1)^1\Pi states. Analysis of this data allows us to predict strong transitions from observed excited levels to the absolute vibronic ground state of RbCs, potentially allowing the production of stable, ultracold polar molecules at rates as large as 10^7 s^{-1}.

Production of Ultracold, Polar RbCs^* Molecules via Photoassociation

We have produced ultracold, polar RbCs* molecules via photoassociation in a laser-cooled mixture of Rb and Cs atoms. Using a model of the RbCs* molecular interaction which reproduces the observed rovibrational structure, we infer decay rates in our experiments into deeply bound X(1)Sigma(+) ground-state RbCs vibrational levels as high as 5 x 10(5) s(-1) per level. Population in such deeply bound levels could be efficiently transferred to the vibrational ground state using a single stimulated Raman transition, opening the possibility to create large samples of stable, ultracold polar molecules.

Enhanced Sensitivity to Variation of m(e)/m(p) in molecular spectra.

We propose new experiments with high sensitivity to a possible variation of the electron-to-proton mass ratio mu identical with m(e)/m(p). We consider a nearly degenerate pair of molecular vibrational levels, each associated with a different electronic potential. With respect to a change in mu, the change in the splitting between such levels can be large both on an absolute scale and relative to the splitting. We demonstrate the existence of such pairs of states in Cs2, where the narrow spectral lines achievable with ultracold molecules make the system promising for future searches for small variations in mu.

Production of Ultracold, PolarRbCs*Molecules via Photoassociation

We have produced ultracold, polar RbCs* molecules via photoassociation in a laser-cooled mixture of Rb and Cs atoms. Using a model of the RbCs* molecular interaction which reproduces the observed rovibrational structure, we infer decay rates in our experiments into deeply bound X(1)Sigma(+) ground-state RbCs vibrational levels as high as 5 x 10(5) s(-1) per level. Population in such deeply bound levels could be efficiently transferred to the vibrational ground state using a single stimulated Raman transition, opening the possibility to create large samples of stable, ultracold polar molecules.

Study of loss in superconducting coplanar waveguide resonators

Superconducting coplanar waveguide (SCPW) resonators have a wide range of applications due to the combination of their planar geometry and high quality factors relative to normal metals. However, their performance is sensitive to both the details of their geometry and the materials and processes that are used in their fabrication. In this paper, we study the dependence of SCPW resonator performance on materials and geometry as a function of temperature and excitation power. We measure quality factors greater than

Inelastic collisions of ultracold heteronuclear molecules in an optical trap.

2\times10^6

Integrated optical addressing of an ion qubit

at high excitation power and

Loading of a surface-electrode ion trap from a remote, precooled source

6\times10^5

Measurement of ion motional heating rates over a range of trap frequencies and temperatures

at a power comparable to that generated by a single microwave photon circulating in the resonator. We examine the limits to the high excitation power performance of the resonators and find it to be consistent with a model of radiation loss. We further observe that while in all cases the quality factors are degraded as the temperature and power are reduced due to dielectric loss, the size of this effect is dependent on resonator materials and geometry. Finally, we demonstrate that the dielectric loss can be controlled in principle using a separate excitation near the resonance frequencies of the resonator.